| Autor: |
Hong, Fan, Kishi, Jocelyn Y., Delgado, Ryan N., Jeong, Jiyoun, Saka, Sinem K., Su, Hanquan, Cepko, Constance L., Yin, Peng |
| Zdroj: |
Nature Methods; February 2024, Vol. 21 Issue: 2 p331-341, 11p |
| Abstrakt: |
Multiplexed fluorescence imaging is typically limited to three- to five-plex on standard setups. Sequential imaging methods based on iterative labeling and imaging enable practical higher multiplexing, but generally require a complex fluidic setup with several rounds of slow buffer exchange (tens of minutes to an hour for each exchange step). We report the thermal-plex method, which removes complex and slow buffer exchange steps and provides fluidic-free, rapid sequential imaging. Thermal-plex uses simple DNA probes that are engineered to fluoresce sequentially when, and only when, activated with transient exposure to heating spikes at designated temperatures (thermal channels). Channel switching is fast (<30 s) and is achieved with a commercially available and affordable on-scope heating device. We demonstrate 15-plex RNA imaging (five thermal × three fluorescence channels) in fixed cells and retina tissues in less than 4 min, without using buffer exchange or fluidics. Thermal-plex introduces a new labeling method for efficient sequential multiplexed imaging. |
| Databáze: |
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